Transcriptional Regulation of IL-10 and Its Cell-Specific Role In Vivo

被引:28
|
作者
MacKenzie, Kirsty F. [1 ]
Pattison, Michael J. [1 ]
Arthur, J. Simon C. [1 ]
机构
[1] Univ Dundee, Coll Life Sci, Div Cell Signaling & Immunol, Dundee DD1 5EH, Scotland
关键词
interleuldn-10; B10; Tr1; macrophage; CREB; STAT3; CD4(+) T-CELLS; STRESS-INDUCED PHOSPHORYLATION; PATTERN-RECOGNITION RECEPTORS; MONOCYTE-DERIVED MACROPHAGES; BRUTONS TYROSINE KINASE; PROTOONCOGENE C-MAF; TOLL-LIKE RECEPTORS; HUMAN B-CELLS; B10; CELLS; INTERLEUKIN-10; RECEPTOR;
D O I
10.1615/CritRevImmunol.2014010694
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IL-10 is an important anti-inflammatory cytokine that plays important roles in controlling inflammatory responses and keeping the immune system in check following activation. Loss of IL-10 function in mice or humans results in the development of inflammatory bowel disease in response to an elevated immune response to the gut flora. IL-10 also acts to prevent excessive inflammation during the course of infection and has been implicated in a variety of autoimmune conditions. In response to inflammatory signals, IL-10 can be produced by a number of immune cells including T cells, B cells, macrophages, and dendritic cells. Distinct mechanisms control the production of IL-10 in these different cells types. In this review, we describe recent studies that have looked at the signaling pathways that regulate IL-10 production in these cells. Given the number of cell types that produce IL-10, it is perhaps not surprising that the in vivo source of IL-10 can vary in different immune models. We also describe how work using conditional IL-10 knockout mice or adoptive transfer of IL-10 deficient cells has begun to further our understanding regarding which specific immune cells are required for IL-10 production in vivo under different conditions.
引用
收藏
页码:315 / 345
页数:31
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